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FDA 510(k)

UNIT, CAUTERY, TEHRMAL,BATTERY-POWERED

K-Number: K030158 · 2003-07-17

ApplicantWalsh Medical Devices, Inc.
Decision Date2003-07-17
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

UNIT, CAUTERY, TEHRMAL,BATTERY-POWERED is the device name listed in this FDA 510(k) record. The listed applicant is Walsh Medical Devices, Inc.. It received FDA 510(k) clearance on 2003-07-17 under 510(k) number K030158. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIT, CAUTERY, TEHRMAL,BATTERY-POWERED?

UNIT, CAUTERY, TEHRMAL,BATTERY-POWERED is a medical device that received FDA 510(k) clearance on 2003-07-17. The listed applicant is Walsh Medical Devices, Inc.. The 510(k) number is K030158.

When did UNIT, CAUTERY, TEHRMAL,BATTERY-POWERED receive FDA 510(k) clearance?

UNIT, CAUTERY, TEHRMAL,BATTERY-POWERED received FDA 510(k) clearance on 2003-07-17, under 510(k) number K030158.

Who is the listed applicant for UNIT, CAUTERY, TEHRMAL,BATTERY-POWERED?

The FDA 510(k) record lists Walsh Medical Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNIT, CAUTERY, TEHRMAL,BATTERY-POWERED?

The FDA product code for UNIT, CAUTERY, TEHRMAL,BATTERY-POWERED is GEI.

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Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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